The Taiwan Food and Drug Administration (TFDA) has been actively engaged in the APEC Regulatory Harmonization Steering Committee (RHSC) to promote the concept of Good Registration Management (GRM). In 2017, TFDA was formally endorsed as the host institution of the APEC GRM Regulatory Science Center of Excellence (CoE). Since then, the CoE host institution has convened annual training activities to promote GRM, which includes Good Review Practice and Good Submission Practice, as well as to foster international cooperation and capacity building among APEC economies.

This year (2026), TFDA continues to host the “2026 APEC GRM CoE Workshop”. The workshop will be held in Chinese Taipei. The host institution of the GRM CoE has designed the program based on the APEC GRM Core Curriculum. In addition, there will be sessions focusing on “AI-Driven Regulatory Review and Reliance in the Generic Drug Lifecycle” and “Special Lecture: Combination Products”. For more details, please refer to the “WORKSHOP AGENDA” section of this web page.

The target participants of this workshop include regulators from authorities, applicants from industry, and researchers in academia who are interested in the GRM of medicinal products. We look forward to your participation. Please register for the workshop on the “WORKSHOP REGISTRATION” page.